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rs863225361

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225361(-;T)
Make rs863225361(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112775681
GeneAPC
is asnp
is mentioned by
dbSNPrs863225361
ClinGenrs863225361
ebirs863225361
HLIrs863225361
Exacrs863225361
Varsomers863225361
Maprs863225361
PheGenIrs863225361
hapmaprs863225361
1000 genomesrs863225361
hgdprs863225361
ensemblrs863225361
gopubmedrs863225361
geneviewrs863225361
scholarrs863225361
googlers863225361
pharmgkbrs863225361
gwascentralrs863225361
openSNPrs863225361
23andMers863225361
23andMe allrs863225361
SNP Nexus

SNPshotrs863225361
SNPdbers863225361
MSV3drs863225361
GWAS Ctlgrs863225361
Max Magnitude0
ClinVar
Risk rs863225361(T;T)
Alt rs863225361(T;T)
Reference Rs863225361(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112111378dupT
CLNSRC
CLNACC RCV000202290.1,